Jinchen C. Li

Xiangya Road 87#
Changsha, 410008, China

Last Updated: 09/26/2026

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Found 154 publications

Corrigendum to "Large-scale profiling of blood microbial signatures in patients with Parkinson's disease and its association with disease progression: a cross-sectional study" [EBioMedicine 126(2026) 106224].

Corrigendum to "Large-scale profiling of blood microbial signatures in patients with Parkinson's disease and its association with disease progression: a cross-sectional study" [EBioMedicine 126(2026) 106224].

Journal: EBioMedicine

Published: June 20, 2026

Haplotype-resolved methylomes reveal parent-of-origin DNA methylation imbalance in autism spectrum disorder.

Haplotype-resolved methylomes reveal parent-of-origin DNA methylation imbalance in autism spectrum disorder.

Journal: Science advances

Published: June 17, 2026

Association of mitochondrial genome variants with Alzheimer's disease in a Chinese population.

Association of mitochondrial genome variants with Alzheimer's disease in a Chinese population.

Journal: Journal of Alzheimer's disease : JAD

Published: May 09, 2026

Metabolomic signatures for diagnosis and clinical severity in Parkinson's disease.

Metabolomic signatures for diagnosis and clinical severity in Parkinson's disease.

Journal: EBioMedicine

Published: January 28, 2026

DeNovoSeer:a deep learning framework for pathogenicity prediction of De novo mutations.

DeNovoSeer:a deep learning framework for pathogenicity prediction of De novo mutations.

Journal: Briefings in bioinformatics

Published: January 14, 2026

Biallelic hexose-6-phosphate dehydrogenase variants cause mitochondrial dysfunction underlying Parkinson's disease.

Biallelic hexose-6-phosphate dehydrogenase variants cause mitochondrial dysfunction underlying Parkinson's disease.

Journal: Science bulletin

Published: January 11, 2026

Genomic landscape of rare variants in a Chinese autism cohort and discovery of novel risk genes.

Genomic landscape of rare variants in a Chinese autism cohort and discovery of novel risk genes.

Journal: Molecular psychiatry

Published: January 05, 2026

Haplotype-resolved long-read sequencing reveals parent-of-origin effects of tandem-repeat variation in autism spectrum disorder.

Haplotype-resolved long-read sequencing reveals parent-of-origin effects of tandem-repeat variation in autism spectrum disorder.

Journal: Science bulletin

Published: December 19, 2025

The genetic spectrum of LRRK2 variants in Parkinson's disease: findings from a large Chinese cohort.

The genetic spectrum of LRRK2 variants in Parkinson's disease: findings from a large Chinese cohort.

Journal: NPJ Parkinson's disease

Published: December 14, 2025

Low-Pass Genome Sequencing Reveals Associations Between Chromosomal Aberrations and Ultrasonographic Anomalies in a Cohort of 19,452 Fetuses.

Low-Pass Genome Sequencing Reveals Associations Between Chromosomal Aberrations and Ultrasonographic Anomalies in a Cohort of 19,452 Fetuses.

Journal: Prenatal diagnosis

Published: November 07, 2025

Short tandem repeat expansions in patients with neurodegenerative dementia.

Short tandem repeat expansions in patients with neurodegenerative dementia.

Journal: EBioMedicine

Published: October 28, 2025

Enhancing interpretation of clinical disease-associated copy number variations from multiple sequencing strategies with CNVSeeker.

Enhancing interpretation of clinical disease-associated copy number variations from multiple sequencing strategies with CNVSeeker.

Journal: Bioinformatics (Oxford, England)

Published: August 28, 2025

Showing 1-12 of 154

Last Updated: 09/26/2026